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Pulmonary Arterial Hypertension: Insights from Genetic Studies

Familial pulmonary arterial hypertension (FPAH) was described 60 years ago, but real progress in understanding its origins and pathogenesis is just beginning. Germline mutations in bone morphogenetic protein receptor type 2 (BMPR2) are responsible for the disease in most families, and also in many s...

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Kaydedildi:
Detaylı Bibliyografya
Yazar: Loyd, James E.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Thoracic Society 2011
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3131832/
https://ncbi.nlm.nih.gov/pubmed/21543793
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1513/pats.201007-047MS
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